Delphine Simon

1.6k total citations · 1 hit paper
13 papers, 1.2k citations indexed

About

Delphine Simon is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Delphine Simon has authored 13 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Delphine Simon's work include Genetic Neurodegenerative Diseases (3 papers), Mitochondrial Function and Pathology (3 papers) and Chromosomal and Genetic Variations (3 papers). Delphine Simon is often cited by papers focused on Genetic Neurodegenerative Diseases (3 papers), Mitochondrial Function and Pathology (3 papers) and Chromosomal and Genetic Variations (3 papers). Delphine Simon collaborates with scholars based in France, Morocco and United States. Delphine Simon's co-authors include Michel Kœnig, Hélène Puccio, Pierre Rustin, Judith Melki, Francesco Danilo Tiziano, C. Hindelang, Mireille Cossée, H. Seznec, Daniel Metzger and Philipp Weber and has published in prestigious journals such as Nature Genetics, Journal of Neuroscience and Human Molecular Genetics.

In The Last Decade

Delphine Simon

13 papers receiving 1.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits

2001 588 citations Hélène Puccio, Delphine Simon et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Delphine Simon France	11	925	630	221	150	134	13	1.2k
Sarn Jiralerspong Canada	13	1.6k 1.7×	1.1k 1.8×	324 1.5×	283 1.9×	138 1.0×	13	1.9k
Marie Wattenhofer‐Donzé France	16	779 0.8×	305 0.5×	158 0.7×	74 0.5×	83 0.6×	19	1.1k
Hiroyuki Ishiura Japan	25	844 0.9×	633 1.0×	177 0.8×	627 4.2×	290 2.2×	146	1.8k
Sonia Ciarmatori Germany	11	629 0.7×	312 0.5×	108 0.5×	94 0.6×	88 0.7×	11	1.0k
Luigi Pianese Italy	16	875 0.9×	822 1.3×	164 0.7×	360 2.4×	78 0.6×	43	1.1k
Christiane Ben Hamida Tunisia	17	901 1.0×	736 1.2×	384 1.7×	427 2.8×	185 1.4×	29	1.6k
Emeline Mundwiller France	13	391 0.4×	316 0.5×	86 0.4×	104 0.7×	155 1.2×	16	738
Norma B. Romero France	22	1.2k 1.3×	291 0.5×	182 0.8×	304 2.0×	168 1.3×	44	1.7k
Barry A. Chioza United Kingdom	20	551 0.6×	182 0.3×	103 0.5×	265 1.8×	222 1.7×	39	1.1k
Takeshi Yaoi Japan	18	530 0.6×	108 0.2×	92 0.4×	55 0.4×	121 0.9×	50	1.1k

Countries citing papers authored by Delphine Simon

Since Specialization

Citations

This map shows the geographic impact of Delphine Simon's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Delphine Simon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Delphine Simon more than expected).

Fields of papers citing papers by Delphine Simon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Delphine Simon. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Delphine Simon. The network helps show where Delphine Simon may publish in the future.

Co-authorship network of co-authors of Delphine Simon

This figure shows the co-authorship network connecting the top 25 collaborators of Delphine Simon. A scholar is included among the top collaborators of Delphine Simon based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Delphine Simon. Delphine Simon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

Grobost, Vincent, Bruno Pereira, A Guilhem, et al.. (2023). Antiplatelet and anticoagulant therapies in hereditary hemorrhagic telangiectasia: A large French cohort study (RETROPLACOTEL). Thrombosis Research. 229. 107–113. 4 indexed citations

Morice‐Picard, Fanny, Giovanni Bénard, Hamid Rezvani, et al.. (2016). Complete loss of function of the ubiquitin ligase HERC2 causes a severe neurodevelopmental phenotype. European Journal of Human Genetics. 25(1). 52–58. 27 indexed citations

Morice‐Picard, Fanny, Eulalie Lasseaux, Dorothée Cailley, et al.. (2013). High‐resolution array‐CGH in patients with oculocutaneous albinism identifies new deletions of the TYR, OCA2, and SLC45A2 genes and a complex rearrangement of the OCA2 gene. Pigment Cell & Melanoma Research. 27(1). 59–71. 21 indexed citations

Simon, Delphine, Thomas Barnetche, Caroline Rooryck, et al.. (2010). A mutation in the 3′-UTR of the HDAC6 gene abolishing the post-transcriptional regulation mediated by hsa-miR-433 is linked to a new form of dominant X-linked chondrodysplasia. Human Molecular Genetics. 19(10). 2015–2027. 77 indexed citations

Rooryck, Caroline, Marianne Stef, Ingrid Burgelin, et al.. (2009). 2.3 Mb terminal deletion in 12p13.33 associated with oculoauriculovertebral spectrum and evaluation of WNT5B as a candidate gene. European Journal of Medical Genetics. 52(6). 446–449. 30 indexed citations

Simon, Delphine, Véronique Veillat, Veronique Guyonnet‐Dupérat, et al.. (2009). Analysis of Post-transcriptional Regulations by a Functional, Integrated, and Quantitative Method. Molecular & Cellular Proteomics. 8(8). 1777–1788. 19 indexed citations

Simon, Delphine, Wallace E. Tyner, & Florence Jacquet. (2009). Economic Analysis of the Potential of Cellulosic Biomass Available in France from Agricultural Residue and Energy Crops. BioEnergy Research. 3(2). 183–193. 25 indexed citations

Stef, Marianne, Delphine Simon, Marie‐Ange Delrue, et al.. (2007). Spectrum of CREBBP gene dosage anomalies in Rubinstein–Taybi Syndrome patients. European Journal of Human Genetics. 15(8). 843–847. 33 indexed citations

Stef, Marianne, Delphine Simon, Ingrid Burgelin, et al.. (2006). Testing and improving experimental parameters for the use of low molecular weight targets in array-CGH experiments. Human Mutation. 27(11). 1143–1150. 2 indexed citations

10.

Simon, Delphine, H. Seznec, Anne Gansmüller, et al.. (2004). Friedreich Ataxia Mouse Models with Progressive Cerebellar and Sensory Ataxia Reveal Autophagic Neurodegeneration in Dorsal Root Ganglia. Journal of Neuroscience. 24(8). 1987–1995. 151 indexed citations

11.

Seznec, H., Delphine Simon, Cécile Bouton, et al.. (2004). Friedreich ataxia: the oxidative stress paradox. Human Molecular Genetics. 14(4). 463–474. 181 indexed citations

12.

Sabot, François, Delphine Simon, & Michel Bernard. (2004). Plant transposable elements, with an emphasis on grass species. Euphytica. 139(3). 227–247. 23 indexed citations

13.

Puccio, Hélène, Delphine Simon, Mireille Cossée, et al.. (2001). Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits. Nature Genetics. 27(2). 181–186. 588 indexed citations breakdown →

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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